| Literature DB >> 15566282 |
Gabriella De Martino1, Giuseppe La Regina, Antonio Coluccia, Michael C Edler, Maria Chiara Barbera, Andrea Brancale, Elizabeth Wilcox, Ernest Hamel, Marino Artico, Romano Silvestri.
Abstract
Several arylthioindoles had excellent activity as inhibitors both of tubulin polymerization and of the growth of MCF-7 human breast carcinoma cells. Methyl 3-[(3,4,5-trimethoxyphenyl)thio]-5-methoxy-1H-indole-2-carboxylate (21), the most potent derivative, showed IC(50) = 2.0 microM, 1.6 times more active than colchicine and about as active as combretastatin A-4 (CSA4). Compound 21 inhibited the growth of the MCF-7 cells at IC(50) = 13 nM. Colchicine and CSA4 had 13 nM and 17 nM IC(50) values, respectively, with these cells.Entities:
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Year: 2004 PMID: 15566282 DOI: 10.1021/jm049360d
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446